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D Rymen

Showing results (1-10 of 4) with videos related to

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Journal of Inherited Metabolic Disease|February 21, 2014
Skin manifestations in CDGD Rymen, J Jaeken
Acta Gastro-Enterologica Belgica|October 13, 2025
Classic galactosemia in the differential diagnosis of neonatal low gammaglutamyltransferase cholestasisT Staut, D Rymen, P Vermeersch, et al.
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A case with rare type of congenital disorder of glycosylation: PGM1-CDGA Küçükçongar, L Tümer, F Süheyl Ezgü, et al.
Journal of Mass Spectrometry : JMS|April 27, 2017
MALDI-MS profiling of serum O-glycosylation and N-glycosylation in COG5-CDGA Palmigiano, R O Bua, R Barone, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Journal of Inherited Metabolic Disease|February 21, 2014
Skin manifestations in CDGD Rymen, J Jaeken
Acta Gastro-Enterologica Belgica|October 13, 2025
Classic galactosemia in the differential diagnosis of neonatal low gammaglutamyltransferase cholestasisT Staut, D Rymen, P Vermeersch, et al.
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A case with rare type of congenital disorder of glycosylation: PGM1-CDGA Küçükçongar, L Tümer, F Süheyl Ezgü, et al.
Journal of Mass Spectrometry : JMS|April 27, 2017
MALDI-MS profiling of serum O-glycosylation and N-glycosylation in COG5-CDGA Palmigiano, R O Bua, R Barone, et al.
Pageof 1